Phase 1 Interstitial Lung Disease Trial, Recruiting NCT06230822 Sponsor: Wuhan Optics Valley Vcanbiopharma Co., Ltd. Condition: Interstitial Lung Disease
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Phase 1 Interstitial Lung Disease Trial, Recruiting

NCT06230822
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You are between 40 and 75 years old (any gender)
  • You have been diagnosed with IPF (idiopathic pulmonary fibrosis) according to specific 2022 medical guidelines
  • Your IPF has been considered stable by your doctor for the past 3 months, and your lung function test results fall within certain specific ranges (confirm with trial site)
  • You have been receiving standard treatment for IPF for at least 3 months and have stayed on that treatment consistently
  • You are willing and able to follow the trial's requirements, complete breathing/lung function tests, and sign a consent form

Who may not be able to join:

  • You are allergic to any ingredient in the trial treatment
  • You have a lung condition other than IPF, such as another type of interstitial lung disease, a lung disease caused by chemicals, drugs, or workplace exposure, a granuloma-related lung disease, or you have had part of a lung surgically removed
  • You currently have or have had asthma, a blood clot in the lungs, a collapsed lung, lung cancer, or an active lung disease; or you have a history of immune system disorders, an immune deficiency condition, or an organ transplant
  • Your recent chest scan (HRCT) shows that the area of air-trapping (emphysema) in your lungs is larger than the area of scarring (fibrosis)
  • You have previously received stem cell therapy, or you are unable to tolerate cell-based treatments
  • Your standard IPF treatment has not been stable in the 3 months before the screening period
  • You have taken certain immune-suppressing or immune-modifying medications (such as Mycophenolate Mofetil, cyclophosphamide, tacrolimus, JAK inhibitors, or certain Chinese herbal medicines) in the past 3 months
  • You have received certain biologic medications (such as rituximab or specific monoclonal antibodies) in the past 6 months
  • You have taken certain other medications including blood thinners or specific drugs used for IPF within the past 4 weeks (confirm with trial site for full list)
  • You have taken part in another interventional clinical trial recently (within 3 months or longer, depending on the drug involved)
  • You have been hospitalised 2 or more times in the past year due to a sudden worsening of your IPF
  • You have had a lung infection in the past month
  • You have previously needed a breathing machine (ventilator), or you currently need to use supplemental oxygen for more than 15 hours per day
  • You have smoked in the past 3 months, or you are unwilling or unable to stop smoking during the trial
  • Your doctor believes your life expectancy may be less than 1 year
  • Your blood test results fall outside certain acceptable ranges for blood cell counts, liver function, kidney function, or other markers (confirm with trial site for specific values)
  • You currently have serious conditions affecting your heart, kidneys, liver, blood, nervous system, or other body systems — for example, severe heart failure, poorly controlled high blood pressure, severe kidney disease requiring dialysis, or advanced liver disease
  • You have or have had any type of cancer (malignant tumour)
  • Your heart tracing (ECG/electrocardiogram) shows certain serious heart rhythm problems
  • You test positive for hepatitis B surface antigen, hepatitis C antibodies, HIV antibodies, or syphilis — though some people with hepatitis B or cured hepatitis C may still be considered eligible (confirm with trial site)
  • You are pregnant, breastfeeding, or have a positive pregnancy test; or you (male or female) are of childbearing potential and are unwilling or unable to use effective non-hormonal contraception during the trial and for 6 months after it ends
  • The investigator (trial doctor) decides for any other reason that the trial is not appropriate for you

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: +86-27-87002897

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Sponsor
Wuhan Optics Valley Vcanbiopharma Co., Ltd.
Registry
ClinicalTrials.gov
Start date
1 February 2024
Est. completion
1 January 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence and severity of cell therapy-related adverse events (AEs) as assessed by CTCAE (V5.0); Maximum tolerated dose (MTD)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov